jolkinolide E

Modify Date: 2025-08-25 12:42:53

jolkinolide E Structure
jolkinolide E structure
Common Name jolkinolide E
CAS Number 54494-34-7 Molecular Weight 300.43500
Density N/A Boiling Point N/A
Molecular Formula C20H28O2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of jolkinolide E


Jolkinolide E is a casbane diterpenoid from the roots of Euphorbia rapulum. Jolkinolide E shows weak selective activity against HepG2, MCF-7, and C6 cell lines[1].

 Names

Name ent-abieta-8(14),13(15)-dien-16,12-olide
Synonym More Synonyms

 jolkinolide E Biological Activity

Description Jolkinolide E is a casbane diterpenoid from the roots of Euphorbia rapulum. Jolkinolide E shows weak selective activity against HepG2, MCF-7, and C6 cell lines[1].
Related Catalog
References

[1]. Liu, Xiao Xue, et al. "Phytochemical Constituents Isolated from Euphorbia rapulum." Chemistry of Natural Compounds 54 (2018): 910-912.

 Chemical & Physical Properties

Molecular Formula C20H28O2
Molecular Weight 300.43500
Exact Mass 300.20900
PSA 26.30000
LogP 4.80100
InChIKey ZXEVPUOHSXARBR-UHFFFAOYSA-N
SMILES CC1=C2C=C3CCC4C(C)(C)CCCC4(C)C3CC2OC1=O

 Synonyms

jolkinolide E
helioscopoindolide G
(4aR,10aR,11aR,11bR)-4,4,8,11b-Tetramethyl-2,3,4,4a,5,6,10a,11,11a,11b-decahydro-1H-10-oxa-cyclopenta[b]phenanthren-9-one
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here



Get all suppliers and price by the below link:

jolkinolide E suppliers

jolkinolide E price

Related Compounds: More...
N-[[(E)-2-methyl-1-phenyl-but-2-enylidene]amino]-2,4-dinitro-aniline
7471-94-5
4-{(E)-[1-(3,5-Dichlorophenyl)-3-methyl-2,5-dioxo-4-imidazolidiny lidene]methyl}benzonitrile
509083-46-9
(Z,E)-2-<(4-methylphenyl)methylene>-3-(2-thienylmethylene)succinic anhydride
100047-13-0
methyl (E)-3-(thiophen-3-yl)acrylate
75754-85-7
methyl (E)-3-methoxybut-2-enoate
4525-28-4
Aegeline
456-12-2
Methyl (E)4.6-dichloro3-(2-oxo-1-phenyl-pyrrolidin-3-ylidenemethyl)-1H-indole-2-carboxylate
166974-21-6
2-[[(E)-1-hydroxy-3-oxo-prop-1-en-2-yl]carbamoyl]benzoic acid
81494-51-1
5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxypyrano[2,3-h]chromen-4-one
113558-13-7
3-[(1R,3S)-2,2-dimethyl-3-(2,2,2-trifluoroacetamido)cyclobutyl]propanoic acid
2679941-93-4
3,3-Dimethyl-1-(2,2,2-trifluoroacetamido)cyclohexane-1-carboxylic acid
2680838-57-5
2-Methyl-3-[1-(2,2,2-trifluoroacetyl)piperidin-3-yl]propanoic acid
2680739-65-3
3-{4-[(Prop-2-en-1-yloxy)carbonyl]morpholin-2-yl}propanoic acid
2680618-06-6
4-Hydroxy-3-{[(prop-2-en-1-yloxy)carbonyl]amino}cyclohexane-1-carboxylic acid
2680761-22-0
2-Methyl-4-{[(prop-2-en-1-yloxy)carbonyl]amino}oxane-4-carboxylic acid
2680619-49-0
rac-(1R,6S)-2-(2,2,2-trifluoroacetyl)-2-azabicyclo[4.2.0]octane-1-carboxylic acid
2679824-06-5
rac-(1R,2R,4S)-2-(2,2,2-trifluoroacetamido)bicyclo[2.2.1]heptane-2-carboxylic acid
2679933-52-7
(1R,5S)-6-(2,2,2-trifluoroacetyl)-6-azabicyclo[3.2.1]octane-5-carboxylic acid
2679812-12-3
rac-(3aR,6aS)-1-(2,2,2-trifluoroacetyl)-octahydrocyclopenta[b]pyrrole-3a-carboxylic acid
2679932-85-3